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Serving leading biopharmaceutical companies globally:

McKesson
Baxter
QuintilesIMS
Boehringer Ingelheim
Julphar
Daiichi Sankyo
Johnson and Johnson
Farmers Insurance
US Department of Justice
Express Scripts

Generated: January 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 071253

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NDA 071253 describes CLONIDINE HYDROCHLORIDE, which is a drug marketed by Exela Pharma Scs Llc, Fresenius Kabi Usa, Hikma Farmaceutica, Luitpold, Zydus Pharms Usa Inc, Actavis Elizabeth, Anchen Pharms, Lupin Ltd, Alembic Pharms Ltd, Am Therap, Aurolife Pharma Llc, Chartwell Molecules, Duramed Pharms Barr, Frontida Biopharm, Impax Labs, Interpharm, Mylan, Par Pharm, Prinston Inc, Sun Pharm Inds Inc, Teva, Unichem, Warner Chilcott, Watson Labs, and Yung Shin Pharm, and is included in fifty-four NDAs. It is available from sixty suppliers. Additional details are available on the CLONIDINE HYDROCHLORIDE profile page.

The generic ingredient in CLONIDINE HYDROCHLORIDE is chlorthalidone; clonidine hydrochloride. There are eighteen drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the chlorthalidone; clonidine hydrochloride profile page.
Summary for 071253
Tradename:CLONIDINE HYDROCHLORIDE
Applicant:Interpharm
Ingredient:clonidine hydrochloride
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength0.2MG
Approval Date:Oct 1, 1986TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Accenture
Daiichi Sankyo
Harvard Business School
Julphar
US Army
Medtronic
Express Scripts
UBS
Dow

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